Thiadiazolidine 1-oxide systems for phosphine-free palladium-mediated catalysis
BR Buckley, SP Neary
Index: Buckley, Benjamin R.; Neary, Stephen P. Tetrahedron, 2010 , vol. 66, # 40 p. 7988 - 7994
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Citation Number: 7
Abstract
We herein report several highly active catalyst systems with thiadiazolidine 1-oxides as ligands for palladium in the Mizoroki–Heck reaction. Excellent yields of stilbenes derived from aryl iodides and bromides have been achieved using as little as 0.00002 mol% catalyst. The ligand/palladium system can be stored as a stock solution open to air at room temperature with no observable loss of activity for a period of several months.
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